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Soluble Tumor Necrosis Factor Receptor Type 2 (sTNF-R2) ELISA Kit

sTNF-R2 Reaktivität: Human Colorimetric Sandwich ELISA 7.8-500 pg/mL Cell Culture Supernatant, Plasma, Serum, Tissue Lysate
Produktnummer ABIN1112690
  • Target Alle Soluble Tumor Necrosis Factor Receptor Type 2 (sTNF-R2) ELISA Kits anzeigen
    Soluble Tumor Necrosis Factor Receptor Type 2 (sTNF-R2)
    Reaktivität
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    Human
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Detektionsbereich
    7.8-500 pg/mL
    Untere Nachweisgrenze
    7.8 pg/mL
    Applikation
    ELISA
    Verwendungszweck
    For quantitative detection of TNFsR ? in human serum, plasma, body fluids, tissue lysates or cell culture supernatants.
    Proben
    Cell Culture Supernatant, Plasma, Serum, Tissue Lysate
    Analytische Methode
    Quantitative
    Sensitivität
    < 2 pg/mL
    Bestandteile
    1. One 96-well plate pre-coated with anti-Human TNFsR2 antibody 2. Lyophilized Human TNFsR2 standards: 2 tubes (10ng / tube) 3. Sample / Standard diluent buffer: 30ml 4. Biotin conjugated anti-Human TNFsR2 antibody (Concentrated): 130 µl.
    Benötigtes Material
    1. 37 °C incubator 2. Microplate reader (wavelength: 450nm) 3. Precise pipette and disposable pipette tips 4. Automated plate washer 5. ELISA shaker 6. 1.5ml of Eppendorf tubes 7. Plate cover 8. Absorbent filter papers 9. Plastic or glass container with volume of above 1L
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  • Kommentare

    This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti-TNFsR ? polyclonal antibody was pre-coated onto 96-well plates. And the biotin conjugated anti-TNFsR? polyclonal antibody was used as detection antibodies. The standards test samples and biotin conjugated detection antibody were added - the wells subsequently and wash with wash buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with wash buffer. TMB substrates were used - visualize HRP enzymatic reaction. TMB was catalyzed by HRP - produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional - the TNFsR? amount of sample captured in plate. Read the O.D. absorbance at 450 nm in a microplate reader and then the concentration of TNFsR? can be calculated.

    Plattentyp
    Pre-coated
    Aufbereitung der Reagenzien
    1. Before the experiment, centrifuge each kit component for several minutes to bring down all reagents to the bottom of tubes. 2. It is recommend to measure each standard and sample in duplicate. 3. Do NOT let the plate completely dry at any time! Since the dry condition can inactivate the biological material on the plate. 4. Do not reuse pipette tips and tubes to avoid cross contamination. 5. Do not use the expired components and the components from different batches. 6. To avoid the marginal effect of plate incubation for temperature differences (the marginal wells always get stronger reaction), it is recommend to equilibrate the ABC working solution and TMB substrate for at least 30 min at room temperature (37°C ) before adding to wells.The TMB substrate (Kit Component 8) is colorless and transparent before use, if not, please contact us for replacement.
    Aufbereitung der Proben

    Preparation of sample and reagents 1. Sample Isolate the test samples soon after collecting, then, analyze immediately (within 2 hours). Or aliquot and store at -20 °C for long term. Avoid multiple freeze-thaw cycles.
    Cell culture supernatants, tissue lysate or body fluids: Centrifuge to remove precipitate, analyze immediately or aliquot and store at -20 °C° C.
    Serum: Coagulate the serum at room temperature (about 4 hours). Centrifuge at approximately 1000 × g for 15 min. Analyze the serum immediately or aliquot and store at -20 °C .
    Plasma: Collect plasma with citrate, heparin or EDTA as the anticoagulant. Centrifuge for 15min at 1000 x g within 30 min of collection. Analyze immediately or aliquot and store frozen at -20 °C. Note: 1. Coagulate blood samples completely, then, centrifuge, and avoid hemolysis and particle. 2. NaN3 can not be used as test sample preservative, since it is the inhibitor for HRP.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konservierungsmittel
    Sodium azide, Thimerosal (Merthiolate)
  • Target Alle Soluble Tumor Necrosis Factor Receptor Type 2 (sTNF-R2) ELISA Kits anzeigen
    Soluble Tumor Necrosis Factor Receptor Type 2 (sTNF-R2)
    Andere Bezeichnung
    sTNF-R2 (sTNF-R2 Produkte)
    Synonyme
    CD120b ELISA Kit, TBPII ELISA Kit, TNF-R-II ELISA Kit, TNF-R75 ELISA Kit, TNFBR ELISA Kit, TNFR1B ELISA Kit, TNFR2 ELISA Kit, TNFR80 ELISA Kit, p75 ELISA Kit, p75TNFR ELISA Kit, TNF-R2 ELISA Kit, TNF-alphaR2 ELISA Kit, TNFRII ELISA Kit, TNFalpha-R2 ELISA Kit, Tnfr-1 ELISA Kit, Tnfr2 ELISA Kit, TNF receptor superfamily member 1B ELISA Kit, tumor necrosis factor receptor superfamily, member 1b ELISA Kit, TNFRSF1B ELISA Kit, Tnfrsf1b ELISA Kit
    Hintergrund
    Tumor necrosis factor receptor superfamily member 1B is a protein that in humans is encoded by the TNFRSF1B gene. This gene contains 10 exons and spans about 26 kb. It is present on many cell types, especially those of myeloid origin, and is strongly expressed on stimulated T and B lymphocytes. It is a member of the Tumor necrosis factor receptor superfamily, which also contains TNFRSF1A. It causes the ubiquitination of TRAF2 by CIAP1, which can play a proapoptotic role in TNF signaling.
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